Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300002M23Rik |
T |
A |
17: 35,879,212 (GRCm39) |
F183L |
possibly damaging |
Het |
4930590J08Rik |
T |
A |
6: 91,921,245 (GRCm39) |
M775K |
probably damaging |
Het |
Actn1 |
T |
G |
12: 80,219,772 (GRCm39) |
I700L |
probably benign |
Het |
Adam5 |
T |
C |
8: 25,276,287 (GRCm39) |
Y460C |
probably damaging |
Het |
Akna |
C |
T |
4: 63,313,502 (GRCm39) |
G207E |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,748,688 (GRCm39) |
H527L |
possibly damaging |
Het |
Anks1 |
C |
A |
17: 28,207,779 (GRCm39) |
N383K |
probably damaging |
Het |
Apba3 |
C |
T |
10: 81,105,204 (GRCm39) |
|
probably null |
Het |
Atp9b |
C |
A |
18: 80,779,308 (GRCm39) |
V1121F |
possibly damaging |
Het |
Bst1 |
A |
G |
5: 43,997,799 (GRCm39) |
D266G |
probably damaging |
Het |
Cep55 |
A |
G |
19: 38,060,202 (GRCm39) |
|
probably null |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Ckb |
T |
C |
12: 111,637,664 (GRCm39) |
K156E |
probably benign |
Het |
Cln3 |
T |
A |
7: 126,174,393 (GRCm39) |
H315L |
probably damaging |
Het |
Cnot6l |
A |
G |
5: 96,227,796 (GRCm39) |
F479S |
probably damaging |
Het |
Col1a1 |
A |
G |
11: 94,837,958 (GRCm39) |
D826G |
unknown |
Het |
Cyp27a1 |
T |
C |
1: 74,774,564 (GRCm39) |
V194A |
probably benign |
Het |
Dis3l2 |
C |
T |
1: 86,971,890 (GRCm39) |
P643S |
probably benign |
Het |
Dpf3 |
T |
C |
12: 83,378,740 (GRCm39) |
D108G |
probably damaging |
Het |
Eif2b4 |
C |
T |
5: 31,350,241 (GRCm39) |
G27D |
probably benign |
Het |
Eif4a1 |
T |
G |
11: 69,563,251 (GRCm39) |
|
probably benign |
Het |
Espl1 |
A |
T |
15: 102,213,372 (GRCm39) |
D566V |
probably damaging |
Het |
Ext2 |
T |
A |
2: 93,644,024 (GRCm39) |
R86* |
probably null |
Het |
Fasn |
A |
T |
11: 120,706,911 (GRCm39) |
F914I |
probably damaging |
Het |
Fbf1 |
A |
G |
11: 116,043,378 (GRCm39) |
L477P |
probably benign |
Het |
Fsd1 |
A |
T |
17: 56,303,452 (GRCm39) |
K441N |
possibly damaging |
Het |
Fsip2 |
T |
A |
2: 82,815,384 (GRCm39) |
S3706T |
probably benign |
Het |
Gabra5 |
A |
T |
7: 57,058,547 (GRCm39) |
N400K |
probably benign |
Het |
Gimap8 |
G |
T |
6: 48,633,068 (GRCm39) |
G296W |
probably damaging |
Het |
Gli2 |
A |
G |
1: 118,763,870 (GRCm39) |
V1427A |
probably benign |
Het |
Gm7334 |
A |
T |
17: 51,005,855 (GRCm39) |
Y47F |
probably damaging |
Het |
Gm8674 |
T |
G |
13: 50,054,791 (GRCm39) |
|
noncoding transcript |
Het |
Gmeb2 |
G |
T |
2: 180,896,039 (GRCm39) |
T377K |
probably benign |
Het |
Gp9 |
T |
A |
6: 87,756,229 (GRCm39) |
D81E |
probably benign |
Het |
Il5ra |
T |
A |
6: 106,715,123 (GRCm39) |
I212F |
possibly damaging |
Het |
Klhl18 |
G |
T |
9: 110,258,029 (GRCm39) |
N470K |
possibly damaging |
Het |
Lfng |
G |
T |
5: 140,598,150 (GRCm39) |
|
probably null |
Het |
Lpo |
A |
G |
11: 87,701,166 (GRCm39) |
I430T |
probably benign |
Het |
Lrrc31 |
C |
T |
3: 30,743,417 (GRCm39) |
D183N |
probably damaging |
Het |
Meis2 |
T |
C |
2: 115,694,893 (GRCm39) |
T410A |
probably benign |
Het |
Myo6 |
A |
G |
9: 80,214,963 (GRCm39) |
D1232G |
probably damaging |
Het |
Ncapd2 |
C |
T |
6: 125,146,803 (GRCm39) |
R1261H |
probably benign |
Het |
Nfkb1 |
C |
T |
3: 135,319,743 (GRCm39) |
V251M |
probably damaging |
Het |
Nmbr |
C |
A |
10: 14,642,730 (GRCm39) |
H96Q |
probably damaging |
Het |
Nop14 |
C |
T |
5: 34,809,737 (GRCm39) |
R256H |
probably damaging |
Het |
Nqo2 |
T |
A |
13: 34,165,501 (GRCm39) |
Y133N |
probably damaging |
Het |
Or1f12 |
T |
C |
13: 21,721,357 (GRCm39) |
I273V |
probably benign |
Het |
Or5w20 |
A |
G |
2: 87,727,157 (GRCm39) |
I213V |
probably benign |
Het |
Pbld2 |
C |
A |
10: 62,888,017 (GRCm39) |
S168R |
probably damaging |
Het |
Pcdhb7 |
G |
T |
18: 37,475,202 (GRCm39) |
G113* |
probably null |
Het |
Pcdhb7 |
G |
T |
18: 37,475,203 (GRCm39) |
G113V |
probably damaging |
Het |
Pdgfra |
A |
T |
5: 75,355,687 (GRCm39) |
T1066S |
probably damaging |
Het |
Prdm8 |
A |
T |
5: 98,332,881 (GRCm39) |
|
probably null |
Het |
Prdm8 |
G |
T |
5: 98,332,882 (GRCm39) |
|
probably null |
Het |
Prkg1 |
T |
C |
19: 30,563,775 (GRCm39) |
Y479C |
probably benign |
Het |
Pudp |
T |
C |
18: 50,701,539 (GRCm39) |
T65A |
probably benign |
Het |
Rbbp6 |
C |
T |
7: 122,598,926 (GRCm39) |
|
probably benign |
Het |
Rcc1 |
C |
G |
4: 132,063,046 (GRCm39) |
V187L |
probably damaging |
Het |
Rims2 |
T |
A |
15: 39,301,124 (GRCm39) |
M285K |
probably damaging |
Het |
Rtkn2 |
T |
C |
10: 67,877,745 (GRCm39) |
*602Q |
probably null |
Het |
Rxfp3 |
T |
G |
15: 11,036,866 (GRCm39) |
S169R |
probably damaging |
Het |
Sardh |
T |
C |
2: 27,118,253 (GRCm39) |
|
probably null |
Het |
Slc24a2 |
A |
T |
4: 87,145,584 (GRCm39) |
F157I |
probably damaging |
Het |
Slc25a20 |
T |
C |
9: 108,559,191 (GRCm39) |
Y186H |
probably damaging |
Het |
Slc25a24 |
A |
G |
3: 109,070,864 (GRCm39) |
R408G |
probably damaging |
Het |
Slc44a5 |
T |
G |
3: 153,959,353 (GRCm39) |
I348S |
probably damaging |
Het |
Slc8a2 |
A |
T |
7: 15,868,100 (GRCm39) |
K111* |
probably null |
Het |
Smc5 |
A |
G |
19: 23,211,367 (GRCm39) |
V589A |
probably damaging |
Het |
Thbd |
A |
T |
2: 148,249,655 (GRCm39) |
I71N |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,605,882 (GRCm39) |
M541T |
probably benign |
Het |
Tie1 |
T |
A |
4: 118,341,968 (GRCm39) |
|
silent |
Het |
Tln1 |
A |
G |
4: 43,547,522 (GRCm39) |
F813S |
possibly damaging |
Het |
Tnrc18 |
A |
T |
5: 142,751,732 (GRCm39) |
L1191* |
probably null |
Het |
Tubb2a |
A |
C |
13: 34,259,240 (GRCm39) |
Y183* |
probably null |
Het |
Ubr4 |
T |
A |
4: 139,123,877 (GRCm39) |
V343E |
probably damaging |
Het |
Vmn2r93 |
A |
T |
17: 18,524,327 (GRCm39) |
D107V |
possibly damaging |
Het |
Vwa5a |
T |
G |
9: 38,647,494 (GRCm39) |
S624R |
probably benign |
Het |
Wwox |
G |
A |
8: 115,433,098 (GRCm39) |
V255I |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,638,804 (GRCm39) |
K546E |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,340,163 (GRCm39) |
F801L |
possibly damaging |
Het |
Zfp407 |
T |
C |
18: 84,577,589 (GRCm39) |
I1175V |
probably benign |
Het |
Zfp646 |
T |
A |
7: 127,480,933 (GRCm39) |
C1037S |
possibly damaging |
Het |
Zfp786 |
A |
T |
6: 47,798,202 (GRCm39) |
C245* |
probably null |
Het |
Zfp827 |
T |
C |
8: 79,787,812 (GRCm39) |
V326A |
probably benign |
Het |
|
Other mutations in Bsn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Bsn
|
APN |
9 |
107,992,309 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00330:Bsn
|
APN |
9 |
107,992,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00863:Bsn
|
APN |
9 |
107,992,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01123:Bsn
|
APN |
9 |
107,993,185 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01330:Bsn
|
APN |
9 |
107,988,112 (GRCm39) |
unclassified |
probably benign |
|
IGL01336:Bsn
|
APN |
9 |
107,988,984 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01399:Bsn
|
APN |
9 |
107,984,386 (GRCm39) |
missense |
unknown |
|
IGL01683:Bsn
|
APN |
9 |
107,992,095 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02022:Bsn
|
APN |
9 |
107,987,617 (GRCm39) |
unclassified |
probably benign |
|
IGL02396:Bsn
|
APN |
9 |
107,993,245 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02538:Bsn
|
APN |
9 |
107,982,435 (GRCm39) |
missense |
unknown |
|
IGL02565:Bsn
|
APN |
9 |
107,990,487 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02661:Bsn
|
APN |
9 |
107,984,135 (GRCm39) |
nonsense |
probably null |
|
IGL02739:Bsn
|
APN |
9 |
107,989,745 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02951:Bsn
|
APN |
9 |
107,992,812 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02987:Bsn
|
APN |
9 |
108,003,503 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03033:Bsn
|
APN |
9 |
107,993,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Bsn
|
APN |
9 |
107,991,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03076:Bsn
|
APN |
9 |
107,982,581 (GRCm39) |
missense |
unknown |
|
R0068:Bsn
|
UTSW |
9 |
107,989,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Bsn
|
UTSW |
9 |
107,989,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Bsn
|
UTSW |
9 |
108,003,185 (GRCm39) |
missense |
probably benign |
0.01 |
R0234:Bsn
|
UTSW |
9 |
107,993,595 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0234:Bsn
|
UTSW |
9 |
107,993,595 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0359:Bsn
|
UTSW |
9 |
107,989,045 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0514:Bsn
|
UTSW |
9 |
108,002,981 (GRCm39) |
missense |
probably benign |
0.07 |
R0593:Bsn
|
UTSW |
9 |
107,987,505 (GRCm39) |
missense |
unknown |
|
R0617:Bsn
|
UTSW |
9 |
107,984,439 (GRCm39) |
missense |
unknown |
|
R0636:Bsn
|
UTSW |
9 |
107,985,033 (GRCm39) |
missense |
unknown |
|
R0652:Bsn
|
UTSW |
9 |
107,982,941 (GRCm39) |
missense |
unknown |
|
R0718:Bsn
|
UTSW |
9 |
107,988,559 (GRCm39) |
unclassified |
probably benign |
|
R0730:Bsn
|
UTSW |
9 |
107,984,011 (GRCm39) |
missense |
unknown |
|
R0905:Bsn
|
UTSW |
9 |
107,982,834 (GRCm39) |
missense |
unknown |
|
R0963:Bsn
|
UTSW |
9 |
107,989,006 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0992:Bsn
|
UTSW |
9 |
107,991,553 (GRCm39) |
nonsense |
probably null |
|
R1101:Bsn
|
UTSW |
9 |
107,993,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1393:Bsn
|
UTSW |
9 |
107,987,716 (GRCm39) |
unclassified |
probably benign |
|
R1490:Bsn
|
UTSW |
9 |
107,991,193 (GRCm39) |
missense |
probably benign |
0.03 |
R1566:Bsn
|
UTSW |
9 |
108,003,184 (GRCm39) |
missense |
probably benign |
0.35 |
R1582:Bsn
|
UTSW |
9 |
107,982,291 (GRCm39) |
missense |
unknown |
|
R1738:Bsn
|
UTSW |
9 |
107,984,133 (GRCm39) |
missense |
unknown |
|
R1867:Bsn
|
UTSW |
9 |
107,983,918 (GRCm39) |
missense |
unknown |
|
R1918:Bsn
|
UTSW |
9 |
107,984,772 (GRCm39) |
missense |
unknown |
|
R1933:Bsn
|
UTSW |
9 |
107,993,643 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1946:Bsn
|
UTSW |
9 |
107,991,850 (GRCm39) |
missense |
probably damaging |
0.99 |
R1978:Bsn
|
UTSW |
9 |
107,991,748 (GRCm39) |
missense |
probably benign |
0.35 |
R2068:Bsn
|
UTSW |
9 |
108,003,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2068:Bsn
|
UTSW |
9 |
107,987,883 (GRCm39) |
unclassified |
probably benign |
|
R2113:Bsn
|
UTSW |
9 |
107,992,085 (GRCm39) |
missense |
probably benign |
0.14 |
R2136:Bsn
|
UTSW |
9 |
107,990,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Bsn
|
UTSW |
9 |
107,987,191 (GRCm39) |
intron |
probably benign |
|
R2266:Bsn
|
UTSW |
9 |
107,992,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2293:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2294:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2368:Bsn
|
UTSW |
9 |
107,988,229 (GRCm39) |
nonsense |
probably null |
|
R2442:Bsn
|
UTSW |
9 |
107,984,119 (GRCm39) |
missense |
unknown |
|
R2507:Bsn
|
UTSW |
9 |
107,993,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R2880:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2881:Bsn
|
UTSW |
9 |
107,990,266 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2922:Bsn
|
UTSW |
9 |
107,992,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R2922:Bsn
|
UTSW |
9 |
107,985,385 (GRCm39) |
missense |
unknown |
|
R3618:Bsn
|
UTSW |
9 |
107,994,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3742:Bsn
|
UTSW |
9 |
107,982,938 (GRCm39) |
missense |
unknown |
|
R3825:Bsn
|
UTSW |
9 |
107,984,055 (GRCm39) |
missense |
unknown |
|
R3982:Bsn
|
UTSW |
9 |
107,984,365 (GRCm39) |
missense |
unknown |
|
R4094:Bsn
|
UTSW |
9 |
107,991,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R4158:Bsn
|
UTSW |
9 |
107,990,145 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4225:Bsn
|
UTSW |
9 |
107,983,932 (GRCm39) |
missense |
unknown |
|
R4261:Bsn
|
UTSW |
9 |
107,987,883 (GRCm39) |
unclassified |
probably benign |
|
R4482:Bsn
|
UTSW |
9 |
107,991,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:Bsn
|
UTSW |
9 |
107,981,277 (GRCm39) |
splice site |
probably null |
|
R4585:Bsn
|
UTSW |
9 |
107,987,662 (GRCm39) |
unclassified |
probably benign |
|
R4628:Bsn
|
UTSW |
9 |
107,990,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4636:Bsn
|
UTSW |
9 |
107,992,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R4679:Bsn
|
UTSW |
9 |
107,987,329 (GRCm39) |
missense |
unknown |
|
R4723:Bsn
|
UTSW |
9 |
107,989,854 (GRCm39) |
missense |
probably benign |
0.03 |
R4843:Bsn
|
UTSW |
9 |
107,984,388 (GRCm39) |
missense |
unknown |
|
R4885:Bsn
|
UTSW |
9 |
107,984,726 (GRCm39) |
nonsense |
probably null |
|
R4942:Bsn
|
UTSW |
9 |
107,983,678 (GRCm39) |
missense |
unknown |
|
R4972:Bsn
|
UTSW |
9 |
107,992,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Bsn
|
UTSW |
9 |
107,992,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5067:Bsn
|
UTSW |
9 |
107,989,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5206:Bsn
|
UTSW |
9 |
107,982,572 (GRCm39) |
missense |
unknown |
|
R5286:Bsn
|
UTSW |
9 |
107,988,123 (GRCm39) |
unclassified |
probably benign |
|
R5492:Bsn
|
UTSW |
9 |
107,989,714 (GRCm39) |
missense |
probably damaging |
0.98 |
R5553:Bsn
|
UTSW |
9 |
107,987,620 (GRCm39) |
unclassified |
probably benign |
|
R5561:Bsn
|
UTSW |
9 |
107,982,710 (GRCm39) |
missense |
unknown |
|
R5597:Bsn
|
UTSW |
9 |
107,992,131 (GRCm39) |
missense |
probably benign |
0.06 |
R5646:Bsn
|
UTSW |
9 |
107,987,631 (GRCm39) |
unclassified |
probably benign |
|
R5796:Bsn
|
UTSW |
9 |
108,003,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Bsn
|
UTSW |
9 |
107,990,208 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5802:Bsn
|
UTSW |
9 |
107,990,208 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5850:Bsn
|
UTSW |
9 |
107,992,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R5938:Bsn
|
UTSW |
9 |
107,990,208 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6221:Bsn
|
UTSW |
9 |
107,982,765 (GRCm39) |
missense |
unknown |
|
R6243:Bsn
|
UTSW |
9 |
107,984,760 (GRCm39) |
missense |
unknown |
|
R6254:Bsn
|
UTSW |
9 |
107,989,065 (GRCm39) |
missense |
probably damaging |
0.96 |
R6263:Bsn
|
UTSW |
9 |
107,990,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:Bsn
|
UTSW |
9 |
107,984,554 (GRCm39) |
missense |
unknown |
|
R6368:Bsn
|
UTSW |
9 |
107,988,513 (GRCm39) |
unclassified |
probably benign |
|
R6574:Bsn
|
UTSW |
9 |
107,991,153 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6793:Bsn
|
UTSW |
9 |
107,991,814 (GRCm39) |
nonsense |
probably null |
|
R6802:Bsn
|
UTSW |
9 |
107,987,823 (GRCm39) |
unclassified |
probably benign |
|
R6943:Bsn
|
UTSW |
9 |
107,985,016 (GRCm39) |
missense |
unknown |
|
R6999:Bsn
|
UTSW |
9 |
107,990,632 (GRCm39) |
missense |
probably benign |
0.00 |
R7149:Bsn
|
UTSW |
9 |
107,993,520 (GRCm39) |
nonsense |
probably null |
|
R7199:Bsn
|
UTSW |
9 |
107,992,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Bsn
|
UTSW |
9 |
108,003,620 (GRCm39) |
nonsense |
probably null |
|
R7349:Bsn
|
UTSW |
9 |
107,987,982 (GRCm39) |
missense |
unknown |
|
R7372:Bsn
|
UTSW |
9 |
107,987,718 (GRCm39) |
missense |
unknown |
|
R7373:Bsn
|
UTSW |
9 |
107,990,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Bsn
|
UTSW |
9 |
108,016,690 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7473:Bsn
|
UTSW |
9 |
107,989,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7482:Bsn
|
UTSW |
9 |
107,990,728 (GRCm39) |
missense |
probably damaging |
0.98 |
R7530:Bsn
|
UTSW |
9 |
107,989,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Bsn
|
UTSW |
9 |
107,992,014 (GRCm39) |
missense |
probably benign |
0.05 |
R7570:Bsn
|
UTSW |
9 |
107,990,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7635:Bsn
|
UTSW |
9 |
107,988,189 (GRCm39) |
missense |
unknown |
|
R7696:Bsn
|
UTSW |
9 |
107,991,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Bsn
|
UTSW |
9 |
107,991,939 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7868:Bsn
|
UTSW |
9 |
107,992,098 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7897:Bsn
|
UTSW |
9 |
107,989,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R7960:Bsn
|
UTSW |
9 |
107,992,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Bsn
|
UTSW |
9 |
107,991,603 (GRCm39) |
missense |
probably benign |
0.01 |
R8056:Bsn
|
UTSW |
9 |
107,982,506 (GRCm39) |
missense |
|
|
R8158:Bsn
|
UTSW |
9 |
107,987,232 (GRCm39) |
missense |
unknown |
|
R8161:Bsn
|
UTSW |
9 |
108,016,729 (GRCm39) |
missense |
probably benign |
0.20 |
R8225:Bsn
|
UTSW |
9 |
107,984,305 (GRCm39) |
missense |
|
|
R8282:Bsn
|
UTSW |
9 |
107,984,890 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8296:Bsn
|
UTSW |
9 |
107,994,578 (GRCm39) |
missense |
probably benign |
0.00 |
R8415:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8417:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8426:Bsn
|
UTSW |
9 |
108,003,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8438:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8439:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8440:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8441:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8442:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8513:Bsn
|
UTSW |
9 |
107,991,709 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8529:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8535:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8546:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8548:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8549:Bsn
|
UTSW |
9 |
107,988,651 (GRCm39) |
missense |
probably benign |
0.00 |
R8682:Bsn
|
UTSW |
9 |
107,983,368 (GRCm39) |
missense |
|
|
R8773:Bsn
|
UTSW |
9 |
107,987,704 (GRCm39) |
missense |
unknown |
|
R8883:Bsn
|
UTSW |
9 |
107,990,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R8906:Bsn
|
UTSW |
9 |
107,984,752 (GRCm39) |
missense |
unknown |
|
R9018:Bsn
|
UTSW |
9 |
107,994,488 (GRCm39) |
missense |
probably benign |
0.06 |
R9070:Bsn
|
UTSW |
9 |
107,987,295 (GRCm39) |
missense |
|
|
R9094:Bsn
|
UTSW |
9 |
107,988,052 (GRCm39) |
missense |
unknown |
|
R9098:Bsn
|
UTSW |
9 |
107,990,173 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9128:Bsn
|
UTSW |
9 |
107,993,349 (GRCm39) |
missense |
probably benign |
0.21 |
R9162:Bsn
|
UTSW |
9 |
107,987,883 (GRCm39) |
missense |
unknown |
|
R9224:Bsn
|
UTSW |
9 |
107,982,686 (GRCm39) |
missense |
|
|
R9230:Bsn
|
UTSW |
9 |
107,989,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Bsn
|
UTSW |
9 |
107,994,289 (GRCm39) |
missense |
probably benign |
0.28 |
R9245:Bsn
|
UTSW |
9 |
107,993,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Bsn
|
UTSW |
9 |
107,988,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Bsn
|
UTSW |
9 |
107,992,993 (GRCm39) |
missense |
probably benign |
0.01 |
R9343:Bsn
|
UTSW |
9 |
107,992,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Bsn
|
UTSW |
9 |
107,993,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Bsn
|
UTSW |
9 |
107,990,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R9378:Bsn
|
UTSW |
9 |
107,984,854 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9408:Bsn
|
UTSW |
9 |
108,016,652 (GRCm39) |
nonsense |
probably null |
|
R9455:Bsn
|
UTSW |
9 |
107,988,531 (GRCm39) |
missense |
unknown |
|
R9563:Bsn
|
UTSW |
9 |
107,984,616 (GRCm39) |
missense |
|
|
R9615:Bsn
|
UTSW |
9 |
107,984,430 (GRCm39) |
missense |
|
|
R9656:Bsn
|
UTSW |
9 |
107,994,407 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:Bsn
|
UTSW |
9 |
107,993,170 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Bsn
|
UTSW |
9 |
107,990,703 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Bsn
|
UTSW |
9 |
108,016,409 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Bsn
|
UTSW |
9 |
108,016,394 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Bsn
|
UTSW |
9 |
107,982,698 (GRCm39) |
missense |
|
|
|